Colon Cancer: Gene >> MUS81

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308110
Start	65863607:65863607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847C>A
AA Mutation	p.His283Asn(p.H283N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308110
Start	65863819:65863819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.977T>C
AA Mutation	p.Leu326Ser(p.L326S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308110
Start	65865266:65865266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768086876
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483His(p.R483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308110
Start	65865026:65865026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282C>A
AA Mutation	p.Leu428Ile(p.L428I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308110
Start	65865035:65865035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763130846
CDS Mutation	c.1291C>T
AA Mutation	p.Arg431Cys(p.R431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308110
Start	65863440:65863440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308110
Start	65865073:65865073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308110
Start	65863877:65863877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112360416
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000308110
Start	65865232:65865232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771900946
CDS Mutation	c.1414C>T
AA Mutation	p.Arg472Ter(p.R472*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MUS81

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308110
Start	65865072:65865072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328C>T
AA Mutation	p.Ala443Val(p.A443V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript